TY - JOUR
T1 - Injecting frequency trajectories and hepatitis C virus acquisition
T2 - Findings from a cohort of people who inject drugs in Montréal, Canada
AU - Fortier, Emmanuel
AU - Høj, Stine Bordier
AU - Sylvestre, Marie-Pierre
AU - Artenie, Andreea Adelina
AU - Minoyan, Nanor
AU - Jutras-Aswad, Didier
AU - Grebely, Jason
AU - Bruneau, Julie
PY - 2021/10
Y1 - 2021/10
N2 - Background: Frequent injecting increases hepatitis C (HCV) acquisition risk among people who inject drugs (PWID). However, few studies have examined how temporal fluctuations in injecting frequency may effect HCV infection risk. Thus, this study examined HCV incidence according to injecting frequency trajectories followed by PWID over one year in Montréal, Canada. Methods: At three-month intervals from March 2011 to June 2016, HCV-uninfected PWID (never infected or cleared infection) enrolled in the Hepatitis Cohort (HEPCO) completed interviewer-administered questionnaires and HCV testing. At each visit, participants reported the number of injecting days (0–30 days) for each of the past three months. In previous work, using group-based trajectory modeling, we identified five injecting frequency trajectories followed by participants over one year (months 1–12 of follow-up), including sporadic, infrequent, increasing, decreasing, and frequent injecting. In this study, we estimated group-specific HCV incidence (months 1–63 of follow-up) using posterior probabilities to assign participants to their most likely trajectory group. Results: Of 386 participants (mean age=40, 82% male, 48% never HCV-infected), 72 acquired HCV during 893 person-years of follow-up. HCV incidence for the whole study sample was 8.1 per 100 person-years (95%CI=6.4–10.1). Trajectory group-specific HCV incidences were highest for those injecting drugs with decreasing (23.9, 14.4–37.5) or increasing frequency (16.0, 10.1–24.3), intermediate for those injecting at consistently high frequency (10.2, 5.4–17.8), and lowest for those injecting infrequently (3.9, 2.2–6.5) or sporadically (4.3, 2.2–7.6). Conclusion: Results suggest that PWID at highest HCV risk are those injecting at high frequency, either transitorily (increasing, decreasing injecting) or consistently (frequent injecting). This study highlights changes in injecting frequency as a potentially important dimension to consider among the factors leading to HCV acquisition. Clinical and public health interventions tailored to PWID with different injecting frequency profiles may contribute to HCV prevention.
AB - Background: Frequent injecting increases hepatitis C (HCV) acquisition risk among people who inject drugs (PWID). However, few studies have examined how temporal fluctuations in injecting frequency may effect HCV infection risk. Thus, this study examined HCV incidence according to injecting frequency trajectories followed by PWID over one year in Montréal, Canada. Methods: At three-month intervals from March 2011 to June 2016, HCV-uninfected PWID (never infected or cleared infection) enrolled in the Hepatitis Cohort (HEPCO) completed interviewer-administered questionnaires and HCV testing. At each visit, participants reported the number of injecting days (0–30 days) for each of the past three months. In previous work, using group-based trajectory modeling, we identified five injecting frequency trajectories followed by participants over one year (months 1–12 of follow-up), including sporadic, infrequent, increasing, decreasing, and frequent injecting. In this study, we estimated group-specific HCV incidence (months 1–63 of follow-up) using posterior probabilities to assign participants to their most likely trajectory group. Results: Of 386 participants (mean age=40, 82% male, 48% never HCV-infected), 72 acquired HCV during 893 person-years of follow-up. HCV incidence for the whole study sample was 8.1 per 100 person-years (95%CI=6.4–10.1). Trajectory group-specific HCV incidences were highest for those injecting drugs with decreasing (23.9, 14.4–37.5) or increasing frequency (16.0, 10.1–24.3), intermediate for those injecting at consistently high frequency (10.2, 5.4–17.8), and lowest for those injecting infrequently (3.9, 2.2–6.5) or sporadically (4.3, 2.2–7.6). Conclusion: Results suggest that PWID at highest HCV risk are those injecting at high frequency, either transitorily (increasing, decreasing injecting) or consistently (frequent injecting). This study highlights changes in injecting frequency as a potentially important dimension to consider among the factors leading to HCV acquisition. Clinical and public health interventions tailored to PWID with different injecting frequency profiles may contribute to HCV prevention.
KW - Cohort study
KW - Hepatitis C virus (HCV)
KW - Injecting frequency
KW - Longitudinal analysis
KW - People who inject drugs (PWID)
KW - Trajectory analysis
UR - http://www.scopus.com/inward/record.url?scp=85114740636&partnerID=8YFLogxK
U2 - 10.1016/j.drugpo.2021.103439
DO - 10.1016/j.drugpo.2021.103439
M3 - Article
C2 - 34518099
AN - SCOPUS:85114740636
SN - 0955-3959
VL - 96
JO - International Journal of Drug Policy
JF - International Journal of Drug Policy
M1 - 103439
ER -